Asx-specific protein ligase

ABSTRACT

The present invention is directed to enzymes having Asx-specific ligase and cyclase activity and to nucleic acids encoding those as well as methods of the manufacture of said enzymes. Further encompassed are methods and uses of these enzymes.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority of U.S. Provisional Patent Application No. 61/983,729 filed Apr. 24, 2014, the contents of which being hereby incorporated by reference in its entirety for all purposes.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is 690148_508D1_SEQUENCE_LISTING.txt. The text file is 457 KB, was created on Feb. 6, 2020, and is being submitted electronically via EFS-Web.

FIELD OF THE INVENTION

The present invention lies in the technical field of enzyme technology and specifically relates to a novel enzyme having Asx-specific ligase and cyclase activity and to nucleic acids encoding those as well as methods of the manufacture of said enzymes. Further encompassed are methods and uses of these enzymes.

BACKGROUND OF THE INVENTION

Head-to-tail macrocyclization of peptides and proteins has been used as a strategy to constrain structures and enhance metabolic stability against proteolytic degradation. In addition, a constrained macrocyclic conformation may also improve pharmacological activity and oral bioavailability. Although most peptides and proteins are produced as linear chains, circular peptides ranging from 6 to 78 residues occur naturally in diverse organisms. These cyclic peptides usually display high resistance to heat denaturation and proteolysis and have inspired a new trend in protein engineering, as demonstrated by recent successes in the cyclization of cytokines, histatin, ubiquitin C-terminal hydrolase, conotoxin and bradykinin-grafted cyclotides. Furthermore, cyclic peptides have been used as therapeutics, including valinomycin, gramicidin S and cyclosporine.

To date chemical methods are typically used for the cyclization of peptides. One possible strategy is native chemical ligation. This method requires an N-terminal cysteine and a C-terminal thioester, requirements that limit its application for non-cysteine-containing peptides. Furthermore, chemical methods are not always feasible, especially for large peptides and proteins.

Although enzymatic methods employing a naturally-occurring cyclase would be ideal, currently only very few peptide cyclases are known and they are for various reasons not fully exploited. However, other enzymes such as sortase A and inteins of which the innate functions are not a cyclase have been applied successfully for cyclization of various peptides and proteins. Nonetheless, these enzymes have shortcomings. Sortase A, for example, is a transpeptidase that anchors surface proteins to bacterial cell wall. Its cyclization reaction usually requires an overnight incubation and 0.1 to 1 molar equivalents of enzyme. Furthermore, sortase A has a pentapeptide recognition sequence LPXTG (SEQ ID NO: 160) and leaves an unnecessary tag on the modified proteins. Inteins are autocatalytic splicing elements that have been used for expression of cyclotides, sunflower trypsin inhibitor, and q-defensin. The intein-mediated cyclization, however, requires genetic fusion of a target protein with the intein domain, a necessity that may affect the protein folding or solubility.

There is thus still need in the art for improved means to cyclize peptides and proteins that overcome the drawbacks of existing technologies and, ideally, are simple, fast and versatile.

SUMMARY OF THE INVENTION

The present invention meets this need by providing a novel Asx-specific protein ligase that meets the above requirements. The inventors have surprisingly found that this enzyme that has been isolated from the medicinal plant Clitoria ternatea is a naturally occurring cyclase that is used as a processing enzyme in the synthesis of cyclotides, a large family of plant cyclic peptides. It has been found that this enzyme is, by far, the fastest known ligase with catalytic activities as high as 542,000 M⁻s⁻¹. It recognizes a tripeptide motif, Asx-His-Val, at the C-terminus, and mediates peptide backbone cyclization by cleaving the sorting sequence His-Val and ligating Asx to the N-terminal residue to form a circular topology. It could be shown that the enzyme does not only efficiently cyclizes cyclotide precursors and various cysteine-rich peptides ranging in sizes from 14 to 58 residues, but also non-cysteine-containing peptides and green fluorescent protein (GFP). This makes it highly versatile and useful in a variety of applications where cyclization of a given peptide or protein is desired.

In a first aspect, the present invention thus relates to an isolated polypeptide comprising or consisting of the amino acid sequence as set forth in SEQ ID NO:1. The polypeptide consisting of the amino acid sequence set forth in SEQ ID NO:1 is also referred to as “butelase 1” herein.

In another aspect, the present invention also relates to nucleic acid molecules encoding the polypeptides described herein, as well as a vector containing such a nucleic acid, in particular a copying vector or an expression vector.

In a further aspect, the invention is also directed to a host cell, preferably a non-human host cell, containing a nucleic acid as contemplated herein or a vector as contemplated herein.

A still further aspect of the invention is a method for manufacturing a polypeptide as described herein, comprising culturing a host cell contemplated herein; and isolating the polypeptide from the culture medium or from the host cell.

In a still further aspect, the present invention relates to the use of polypeptides described herein for protein ligation, in particular for cyclizing one or more peptide(s).

Another aspect of the invention is directed to the use of polypeptides that comprise or consist of

-   -   (i) any one of the amino acid sequences as set forth in SEQ ID         Nos:3-109;     -   (ii) an amino acid sequence that shares at least 60, preferably         at least 70, more preferably at least 80, most preferably at         least 90% sequence identity with any one of the amino acid         sequences of (i) over its entire length;     -   (iii) an amino acid sequence that shares at least 80, preferably         at least 90, more preferably at least 95% sequence homology with         any one of the amino acid sequences of (i) over its entire         length; or     -   (iv) a fragment of any one of (i)-(iii),         for ligating at least two peptides or cyclizing a peptide.

In still another aspect, the invention relates to a method for cyclizing a peptide, the method comprising incubating said peptide with the polypeptides described above in connection with the inventive uses under conditions that allow cyclization of said peptide.

In a still further aspect, the invention relates to a method for ligating at least two peptides, the method comprising incubating said peptides with the polypeptides described above in connection with the inventive uses under conditions that allow ligation of said peptides.

In another aspect, the invention relates to a solid support material onto which the isolated polypeptides of the invention are immobilized as well as the use thereof and methods that use such substrates.

In another aspect, the invention also encompasses a transgenic plant comprising a nucleic acid molecule encoding a polypeptide having protein ligase and/or cyclase activity as described herein. The polypeptide is preferably not naturally present in said plant. Accordingly, the present invention also features transgenic plants that express a heterologous polypeptide according to the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the oxidative folding of kB1-NHV (SEQ ID NO: 110). The peptide was folded for 18 h at a 30 μM concentration in buffer containing 50% acetonitrile, 100 mM ammonium bicarbonate, 3 mM reduced glutathione, pH 8.0. The folded peptide eluted last in the RP-HPLC.

FIG. 2 shows the MS characterization of peptide cyclase activity. (a) Schematic illustration of kB1-NHV cyclization mediated by butelase 1. Residues at the recognition site of butelase 1 (P1, P1′ and P2′) are labeled. (b,c) MS profiles of kB1-NHV cyclization mediated by the crude extract of C. ternatea and purified butelase 1, respectively. Peptides in the bracket are cliotides, naturally occurring cyclotides in C. ternatea. The product, cyclic kB1, is indicated by the arrows.

(d) Jack bean legumain was used as a control. MS profile shows that jack beak legumain hydrolyzed the asparaginyl bond in kB1-NHV to give linear form of kB1. Peaks labeled with K⁺ or K₂ ⁺ are ion adducts corresponding to the binding of one or two potassium ions, respectively.

FIG. 3 shows the co-elution of enzyme-cyclized kB1 and native peptide. (a) HPLC profile of enzyme-cyclized kB1. (b) HPLC profile of native kB1 extracted from O. affinis. (c) Co-elution profile of enzyme-cyclized and native kB1.

FIG. 4 shows MS evidence of a cyclic backbone in the enzyme-cyclized kB1 obtained from conversion of kB1-NHV by butelase 1. (a) MS profile of the cyclized kB1 after S-carbamido methylation. The cyclized kB1 has a m/z value of 2891, which became 3239 after S-alkylation. A minor peak at 3182 is observed due to incomplete alkylation where only 5 cysteines were modified. (b) MS profile of S-alkylated kB1 after tryptic digestion. A mass increase of 18 Da was observed, which indicated the addition of a water molecule and a cyclic backbone. (c) MS/MS profile of the 3257-Da tryptic fragment. The peptide sequence is shown at the top of the MS/MS spectrum. The y-ions are labeled at the top of corresponding peaks.

FIG. 5 shows 1D NMR spectra comparison of enzyme-cyclized kB1 (dark grey) and native kB1 (light grey). Peptides were dissolved in 95% H₂O/5% D₂O at pH 4.3. The spectra were recorded at 298 K.

FIG. 6 shows isolation, characterization and homology modeling of butelase 1. (a) SDS-PAGE analysis of purified butelase 1. Proteins were visualized by silver staining. The left lane is purified butelase 1 and the right lane is a protein ladder with molecular weights (kDa) indicated. (b) Labeling of butelase 1 by the legumain-specific probe LP-1. Proteins were resolved by SDS-PAGE and visualized by a Typhoon scanner (GE Health Care) with a Cy5 filter. (c) Translated sequence of butelase 1 precursor (SEQ ID NO: 2) deduced from the EST sequences. The sequence is color-coded with the endoplasmic reticulum signal shown in black, N-terminal prodomain in orange, the AEP domain in blue, the active peptide region in magenta, and the LSAM domain in gray. The first and the last residues (V42 and N383) of the purified active enzyme are labeled. The conserved residues of the catalytic triad (Asn59, His165 and Cys207) are italic. Peptide sequences obtained from the in-gel tryptic digestion are underlined. (d)Modeling structure of zymogenic butelase 1 based on the structure of human legumain. The left panel shows the modeled zymogenic butelase 1 with the AEP domain shown in blue, active peptide region in magenta and LSAM domain in gray. The top-right panel shows the structure alignment of modeled butelase 1 and the template human legumain (PDB ID: 4FGU; yellow). The catalytic triad residues (Asn59, His165 and Cys207) are highlighted in red sticks within the black dashed box, and an enlarged view in the bottom-right panel.

FIG. 7 shows the protein identification of butelase 1 by in-gel tryptic digestion. Five dominant tryptic fragments were sequenced by MS/MS and are shown at the top of the MS profile.

FIG. 8 shows the chemical structure of the leguman specific probe LP-1.

FIG. 9 shows the kinetic characterization of butelase 1 as a peptide cyclase. (a) RP-HPLC traces of the cyclization reaction over a time course of 45 min. The substrate kB1-NHV and the product kB1 are labeled. The assays were performed at 37° C. in the presence of 0.125 μM butelase 1 and 50 μM kB1-NHV. The absorbance was monitored at a wavelength of 220 nm. (b-d) Michaelis-Menten plots of butelase 1 kinetics for kB1-NHV (SEQ ID NO: 110), SFTI-NHV (SEQ ID NO: 135) and SA-kB1-NHV. The cyclization rates were calculated by converting the HPLC-peak areas of the products into concentrations. For the kinetic measurements of kB1-NHV (SEQ ID NO: 110) and SFTI-NHV (SEQ ID NO: 135), the assays were performed at 37° C. for 12 min in the presence of 0.125 μM butelase 1 and varying substrate concentrations. For SA-kB1-NHV, due to much faster cyclization rate, the enzyme concentration was used at 5 nM instead of 0.125 μM and the incubation time was reduced to 6 min.

FIG. 10 shows cyclodimer formation of kB1. (a) RP-HPLC profile illustrates the cyclodimer formation of kB1. The reaction was performed at 37° C., for 4 h in the presence of 0.125 μvM butelase 1 and 500 μM kB1-NHV. Peak 1 is the isomer of kB1 with the same m/z value of 2891 as native cyclic kB1. Peak 2 has the m/z value of 2893, which indicates the reduction of one disulfide bond of kB1. The substrate kB1-NHV and the products, kB1 and (kB1)₂ are labeled at peak apex. (b) MS profile illustrates the cyclodimer formation of kB1 (SEQ ID NO: 139). Peak labeled with K⁺ is the potassium adduct.

FIG. 11 shows MS profiles of kB1-NHV truncated analogs after treatment with butelase 1. Assays were performed at 37° C. for 30 h in the presence of 0.125 μM butelase 1 and 50 μM of each substrate. (a) MS profile of kB1-NH treated with butelase 1. (b) MS profile of kB1-N* treated with butelase 1. The kB1 product and truncated analogs, kB1-NH and kB1-N*, were labeled at the peak apex. The peak with an m/z value of 2969.4 represents a modified cyclic kB1 where one cysteine residue is S-alkylated with β-ME. Peaks labeled with K⁺ and K₂ ⁺ are ion adducts that correspond to the binding of one or two potassium ions, respectively.

FIG. 12 shows MS profiles of the kB1-NHV analogs after treatment with butelase 1. (a-d) The conserved Asn at the P1 position was replaced by Glu, Gln, Ala or Asp residues in the kB1-NHV substrate. Assays were performed at 37° C. for 4 h in the presence of 0.125 pM butelase 1 and 50 μM of each substrate. The masses of the kB1-NHV analogs are labeled at the peak apex. In the case of kB1-DHV, a cyclized product was observed with an m/z value of 2892. Peaks labeled with K⁺ and K₂ ⁺ are ion adducts that correspond to the binding of one or two potassium ions, respectively.

FIG. 13 shows HPLC profiles of Z-AAN-AMC treatment with jack bean legumain and butelase 1. (a) HPLC trace of Z-AAN-AMC as a control. (b) HPLC trace showing the hydrolyzed product 7-amino-4-methylcoumarin catalyzed by jack bean legumain. The assay was performed at 37° C. for 30 h in the presence of 8 μU jack bean legumain and 50 μM Z-AAN-AMC. (c) HPLC trace showing the effect of butelase 1 on Z-AAN-AMC. The assay was performed at 37° C. for 30 h in the presence of 0.125 μM butelase 1 and 50 μM Z-AAN-AMC. No significant hydrolyzed product (indicated by the arrow) was observed after 30 h incubation. The absorbance was monitored at a wavelength of 254 nm.

FIG. 14 shows HPLC profiles of SA-pyroGlu-kB1-NHV ligation with GIGGIR(SEQ ID NO:123). (a) HPLC trace of SA-pyroGlu-kB1-NHV as a control. (b) HPLC trace showing the hydrolyzed product SA-pyroGlu-kB1-N in the absence of butelase 1. (c) HPLC trace showing the ligation reaction in the presence of 5 time excess of GIGGIR (SEQ ID NO: 123) (250 pM). (d) HPLC trace showing the ligated reaction in the presence of 20 time excess of GIGGIR (SEQ ID NO: 123) (1 mM). The ligation reactions were performed at 37° C. for 20 min in the presence of 0.125 μM butelase 1 and 50 μM SA-pyroGlu-kB1-NHV and varying concentration of GIGGIR (SEQ ID NO: 123) (0-1 mM).

FIG. 15 shows the acceptor specificity of butelase-mediated peptide ligation. (a) Intermolecular ligation of KALVINHV (SEQ ID NO:122) and XIGGIR (SEQ ID NO:123) facilitated by butelase 1. The reactions were performed in the presence of 100 nM butelase 1, 100 μM KALVINHV (SEQ ID NO: 122) and 1 mM XIGGIR (SEQ ID NO: 123) and incubated for 10 min or 2 h. The ligation yields were calculated by converting the HPLC peak area into concentration. (b) Intermolecular ligation of KALVINHV (SEQ ID NO: 122) and LXGGIR (SEQ ID NO: 124) facilitated by butelase 1. The reactions were performed in the presence of 100 nM butelase 1, 100 μM KALVINHV (SEQ ID NO: 122) and 1 mM LXGGIR (SEQ ID NO: 124) and incubated for 10 min or 2 h. The ligation yields were calculated by converting the HPLC peak area into concentration.

FIG. 16 shows the butelase mediated cyclization of human neuromedin U, salusin a, apelin and galanin and rat neuromedin U. The cyclization reactions were performed in 50 μl reaction mixtures containing 50 μM peptides and 0.1 μM butelase 1 (0.002 molar equivalent) at 37° C. and monitored by MS.

FIG. 17 shows the butelase mediated cyclization of a modified GFP ending with Asn-His-Val motif at the C-terminus and starting with Gly-Ile at the N-terminus. The cyclization reaction was carried in the presence of 25 μM GFP and 0.1 μM butelase 1 (0.004 molar equivalent). The cyclization reaction was monitored by high resolution ESI-MS.

FIG. 18 shows the butelase mediated ligation of GFP with a short peptide GIGK(biotin)R (SEQ ID NO:134). The ligation reaction was performed at 37° C. for 30 minutes in the presence of 0.125 μM butelase 1, 50 μM GFP and 1mM of the peptide substrate and monitored by MS.

FIG. 19 shows the mass spectrometry profile of ligation between the fluorescently labelled peptide GIR-AMC (AMC=7-amino-4-methylcoumarin) and (a) ABL-Mono and (b) ERK-Darp for 20 minute incubation. 7232 and 7354.8 are the peaks of ABL-Mono and its ligated product protonated once. 10251.4 and 6031.3 are the peaks of ERK-Darp ligated product protonated once and twice.

FIG. 20 shows the ESI-MS profiles of (a,c) ERK-Darp and GFP-NHV substrate as the negative controls, (b,d) 50 μM ERK-Darp and 50 μM GFP-NHV incubated with 1 mM FITC-GKNHV (SEQ ID NO: 150) and 50nM butelase 1 for 10 minute at 42° C.

FIG. 21 shows the HPLC and MS profiles of ligation between an ubiquitin (SEQ ID NO:148) and the peptide YKN-thioglycolic acid-V.

FIG. 22 shows the analysis of butelase 1-mediated dimerization. (a) Structure of G2K dimeric core peptide, (b) and (c) structures of the two different possible mono-ligated G2K peptide (SEQ ID NO: 162), (d) structure of the fully ligated dimer peptide (SEQ ID NO: 163). (e) Mass spectrometry analysis of the dimerization reaction shows the presences of both the mono-ligated and fully ligated dimer (SEQ ID NOS: 125, 162 and 163) respectively.

FIG. 23 shows the acceptor specificity of butelase-mediated peptide cyclization. The reactions were performed in the presence of 50 nM butelase 1, 50 μM peptide and incubated for 60 min at 42° C. The cyclization yields were calculated by converting the HPLC peak area into concentration. (a) Intramolecular cyclization of XLYRRGRYLRRNHV (SEQ ID NO:157) facilitated by butelase 1. (b) Intramolecular ligation of XRLYRGRYLRRNHV (SEQ ID NO:158) facilitated by butelase 1. (c) Intramolecular ligation of GXLYRGRYLRRNHV (SEQ ID NO:159) facilitated by butelase 1.

FIG. 24 shows cyclisation assays of peptide substrates (a) conotoxin GV-17 (SEQ ID NO: 111), (b) SFTI-NHV (SEQ ID NO: 135) and (c) kalata B1-NHV (SEQ ID NO: 110) by butelase 1 immobilized onto ProSwift ConA-1S affinity column.

DETAILED DESCRIPTION

The present invention is based on the inventors' identification of a peptide ligase/cyclase enzyme isolated from Clitoria ternatea that is capable of ligating/cyclizing peptides with very high catalytic activities. It recognizes a tripeptide motif, Asx-His-Val, at the C-terminus, and mediates peptide backbone cyclization by cleaving the sorting sequence His-Val and ligating Asx to the N-terminal residue to form a circular topology. Significantly, the enzyme can not only efficiently cyclizes cyclotide precursors and various cysteine-rich peptides ranging in sizes from 14 to 58 residues, but also non-cysteine-containing peptides and proteins, such as green fluorescent protein (GFP). This makes it highly versatile and useful in a variety of applications where cyclization of a given peptide or protein is desired.

The invention, in a first aspect, covers said enzyme in isolated form and, more specifically, is directed to an isolated polypeptide comprising, consisting essentially of or consisting of the amino acid sequence as set forth in SEQ ID NO:1. The polypeptide consisting of the amino acid sequence set forth in SEQ ID NO:1 is also referred to as “butelase 1” herein. “Isolated”, as used herein, relates to the polypeptide in a form where it has been at least partially separated from other cellular components it may naturally occur or associate with. The polypeptide may be a recombinant polypeptide, i.e. polypeptide produced in a genetically engineered organism that does not naturally produce said polypeptide.

A polypeptide according to the present invention exhibits protein ligation activity, i.e. it is capable of forming a peptide bond between two amino acid residues, with these two amino acid residues being located on the same or different peptides or proteins, preferably on the same peptide or protein so that said ligation activity cyclizes said peptide or protein. Accordingly, in various embodiments, the polypeptide of the invention has cyclase activity. In various embodiments, this protein ligation or cyclase activity also includes an endopeptidase activity, i.e. the polypeptide form a peptide bond between two amino acid residues and at the same time cleaves an existing peptide bond. This means that cyclization need not to occur between the termini of a given peptide but can also occur between internal amino acid residues, with the amino acids C-terminal or N-terminal to the amino acid used for cyclization being cleaved off. In a preferred embodiment, the polypeptide forms a cyclized peptide by ligating the N-terminus to an internal amino acid and cleaving the remaining C-terminal amino acids.

The polypeptide as disclosed herein is “Asx-specific” in that the amino acid C-terminal to which ligation occurs, i.e. the C-terminal end of the peptide that is ligated, is either asparagine (Asn or N) or aspartic acid (Asp or D), preferably asparagine. In various embodiments, a polypeptide according to the present invention also has ligation activity for a peptide that has a C-terminal Asx (N or D) residue that is amidated, i.e. the C-terminal carboxy group is replaced by an amide group. This amide group is cleaved off in the course of the ligation reaction. Accordingly, such amidated peptide substrates, while still being ligated/cyclized, do not comprise the naturally occurring tripeptide motif NHV.

“Polypeptide”, as used herein, relates to polymers made from amino acids connected by peptide bonds. The polypeptides, as defined herein, can comprise 50 or more amino acids, preferably 100 or more amino acids. “Peptides”, as used herein, relates to polymers made from amino acids connected by peptide bonds. The peptides, as defined herein, can comprise 2 or more amino acids, preferably 5 or more amino acids, more preferably 10 or more amino acids, for example 10 to 50 amino acids.

In various embodiments, the polypeptide comprises or consists of an amino acid sequence that is at least 60%, 65%, 70%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 99%, 99.25%, or 99.5% identical or homologous to the amino acid sequence set forth in SEQ ID NO:1 over its entire length. In some embodiments, it has an amino acid sequence that shares at least 60, preferably at least 70, more preferably at least 80, most preferably at least 90% sequence identity with the amino acid sequence set forth in SEQ ID NO:1 over its entire length or has an amino acid sequence that shares at least 80, preferably at least 90, more preferably at least 95% sequence homology with the amino acid sequence set forth in SEQ ID NO:1over its entire length.

In various embodiments, the polypeptide may be a precursor of the mature enzyme. In such embodiments, it may comprise or consist of the amino acid sequence set forth in SEQ ID NO:2. Also encompassed are polypeptides having an amino acid sequence that is at least 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 99%, 99.25%, or 99.5% identical or homologous to the amino acid sequence set forth in SEQ ID NO:2 over its entire length.

The identity of nucleic acid sequences or amino acid sequences is generally determined by means of a sequence comparison. This sequence comparison is based on the BLAST algorithm that is established in the existing art and commonly used (cf. for example Altschul et al. (1990) “Basic local alignment search tool”, J. Mol. Biol. 215:403-410, and Altschul et al. (1997): “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs”; Nucleic Acids Res., 25, p. 3389-3402)and is effected in principle by mutually associating similar successions of nucleotides or amino acids in the nucleic acid sequences and amino acid sequences, respectively. A tabular association of the relevant positions is referred to as an “alignment.” Sequence comparisons (alignments), in particular multiple sequence comparisons, are commonly prepared using computer programs which are available and known to those skilled in the art.

A comparison of this kind also allows a statement as to the similarity to one another of the sequences that are being compared. This is usually indicated as a percentage identity, i.e. the proportion of identical nucleotides or amino acid residues at the same positions or at positions corresponding to one another in an alignment. The more broadly construed term “homology”, in the context of amino acid sequences, also incorporates consideration of the conserved amino acid exchanges, i.e. amino acids having a similar chemical activity, since these usually perform similar chemical activities within the protein. The similarity of the compared sequences can therefore also be indicated as a “percentage homology” or “percentage similarity.” Indications of identity and/or homology can be encountered over entire polypeptides or genes, or only over individual regions. Homologous and identical regions of various nucleic acid sequences or amino acid sequences are therefore defined by way of matches in the sequences. Such regions often exhibit identical functions. They can be small, and can encompass only a few nucleotides or amino acids. Small regions of this kind often perform functions that are essential to the overall activity of the protein. It may therefore be useful to refer sequence matches only to individual, and optionally small, regions. Unless otherwise indicated, however, indications of identity and homology herein refer to the full length of the respectively indicated nucleic acid sequence or amino acid sequence.

In various embodiments, the polypeptide described herein comprises the amino acid residue N at the position corresponding to position 19 of SEQ ID NO:1; and/or the amino acid residue H at the position corresponding to position 124 of SEQ ID NO:1; and/or the amino acid residue C at the position corresponding to position 166 of SEQ ID NO:1. It has been found that these amino acid residues putatively play a role in the catalytic activity of the polypeptide. In preferred embodiments, the polypeptides thus comprise at least two, more preferably all three of the above indicated residues at the given or corresponding positions.

The isolated polypeptides of the present invention preferably have enzymatic activity, in particular protein ligase, preferably cyclase activity. In various embodiments, this means that they can ligate a given peptide with an efficiency of 80% or more, preferably 90% or more. The protein ligation, preferably cyclization, reaction is preferably comparably fast, i.e. said polypeptide can cyclize a given peptide with a K_(m) of 500

M or less, preferably 250

M or less; and/or a k_(cat) of at least 0.05 s⁻¹, preferably at least 0.5 s⁻¹, more preferably at least 1.0 s⁻¹, most preferably at least 1.5 s⁻¹. Preferred polypeptides satisfy both requirements, i.e. the K_(m) and k_(cat) requirement. Methods to determine such Michaelis-Menten kinetics are well known in the art and can be routinely applied by those skilled in the art. It is preferred that the polypeptides of the invention have at least 50%, more preferably at least 70, most preferably at least 90% of the protein ligase activity of the enzyme having the amino acid sequence of SEQ ID NO:1.

Polypeptides according to the embodiments described herein can comprise amino acid modifications, in particular amino acid substitutions, insertions, or deletions. Such polypeptides are, for example, further developed by targeted genetic modification, i.e. by way of mutagenesis methods, and optimized for specific purposes or with regard to special properties (for example, with regard to their catalytic activity, stability, etc.). In addition, nucleic acids contemplated herein can be introduced into recombination formulations and thereby used to generate entirely novel protein ligases, cyclases or other polypeptides.

In various embodiments, the polypeptides having ligase/cyclase activity may be posttranslationally modified, for example glycosylated. Such modification may be carried out by recombinant means, i.e. directly in the host cell upon production, or may be achieved chemically or enzymatically after synthesis of the polypeptide, for example in vitro.

The objective may be to introduce targeted mutations, such as substitutions, insertions, or deletions, into the known molecules in order, for example, to alter substrate specificity and/or improve the catalytic activity. For this purpose, in particular, the surface charges and/or isoelectric point of the molecules, and thereby their interactions with the substrate, can be modified. Alternatively or additionally, the stability of the polypeptide can be enhanced by way of one or more corresponding mutations, and its catalytic performance thereby improved. Advantageous properties of individual mutations, e.g. individual substitutions, can supplement one another.

In various embodiments, the polypeptide may be characterized in that it is obtainable from a polypeptide as described above as an initial molecule by single or multiple conservative amino acid substitution. The term “conservative amino acid substitution” means the exchange (substitution) of one amino acid residue for another amino acid residue, where such exchange does not lead to a change in the polarity or charge at the position of the exchanged amino acid, e.g. the exchange of a nonpolar amino acid residue for another nonpolar amino acid residue. Conservative amino acid substitutions in the context of the invention encompass, for example, G=A=S, I−V=L=M, D=E, N=Q, K=R, Y=F, S=T, G=A=I=V=L=M=Y=F=W=P=S=T.

Alternatively or additionally, the polypeptide may be characterized in that it is obtainable from a polypeptide contemplated herein as an initial molecule by fragmentation or by deletion, insertion, or substitution mutagenesis, and encompasses an amino acid sequence that matches the initial molecule over a length of at least 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 325, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, or 342 continuously connected amino acids. It is preferred that in such embodiments, the amino acids N19, H124 and C166 contained in the initial molecule are still present.

In various embodiments, the present invention thus also relates to fragments of the polypeptides described herein, with said fragments retaining enzymatic activity. It is preferred that they have at least 50%, more preferably at least 70, most preferably at least 90% of the protein ligase and/or cyclase activity of the initial molecule, preferably of the polypeptide having the amino acid sequence of SEQ ID NO:1. The fragments are preferably at least 150 amino acids in length, more preferably at least 200 or 250, most preferably at least 300. It is further preferred that these fragments comprise the amino acids N, H and C at positions corresponding to positions 19, 124 and 166 of SEQ ID NO:1. Preferred fragments therefore comprise amino acids 19-166, more preferably 10-200, most preferably 1-277 of the amino acid sequence set forth in SEQ ID NO:1.

The nucleic acid molecules encoding the polypeptides described herein, as well as a vector containing such a nucleic acid, in particular a copying vector or an expression vector also form part of the present invention.

These can be DNA molecules or RNA molecules. They can exist as an individual strand, as an individual strand complementary to said individual strand, or as a double strand. With DNA molecules in particular, the sequences of both complementary strands in all three possible reading frames are to be considered in each case. Also to be considered is the fact that different codons, i.e. base triplets, can code for the same amino acids, so that a specific amino acid sequence can be coded by multiple different nucleic acids. As a result of this degeneracy of the genetic code, all nucleic acid sequences that can encode one of the above-described polypeptides are included in this subject of the invention. The skilled artisan is capable of unequivocally determining these nucleic acid sequences, since despite the degeneracy of the genetic code, defined amino acids are to be associated with individual codons. The skilled artisan can therefore, proceeding from an amino acid sequence, readily ascertain nucleic acids coding for that amino acid sequence. In addition, in the context of nucleic acids according to the present invention one or more codons can be replaced by synonymous codons. This aspect refers in particular to heterologous expression of the enzymes contemplated herein. For example, every organism, e.g. a host cell of a production strain, possesses a specific codon usage. “Codon usage” is understood as the translation of the genetic code into amino acids by the respective organism. Bottlenecks in protein biosynthesis can occur if the codons located on the nucleic acid are confronted, in the organism, with a comparatively small number of loaded tRNA molecules. Also it codes for the same amino acid, the result is that a codon becomes translated in the organism less efficiently than a synonymous codon that codes for the same amino acid. Because of the presence of a larger number of tRNA molecules for the synonymous codon, the latter can be translated more efficiently in the organism.

By way of methods commonly known today such as, for example, chemical synthesis or the polymerase chain reaction (PCR) in combination with standard methods of molecular biology or protein chemistry, a skilled artisan has the ability to manufacture, on the basis of known DNA sequences and/or amino acid sequences, the corresponding nucleic acids all the way to complete genes. Such methods are known, for example, from Sambrook, J., Fritsch, E. F., and Maniatis, T, 2001, Molecular cloning: a laboratory manual, 3rd edition, Cold Spring Laboratory Press.

“Vectors” are understood for purposes herein as elements—made up of nucleic acids—that contain a nucleic acid contemplated herein as a characterizing nucleic acid region. They enable said nucleic acid to be established as a stable genetic element in a species or a cell line over multiple generations or cell divisions. In particular when used in bacteria, vectors are special plasmids, i.e. circular genetic elements. In the context herein, a nucleic acid as contemplated herein is cloned into a vector. Included among the vectors are, for example, those whose origins are bacterial plasmids, viruses, or bacteriophages, or predominantly synthetic vectors or plasmids having elements of widely differing derivations. Using the further genetic elements present in each case, vectors are capable of establishing themselves as stable units in the relevant host cells over multiple generations. They can be present extrachromosomally as separate units, or can be integrated into a chromosome resp. into chromosomal DNA.

Expression vectors encompass nucleic acid sequences which are capable of replicating in the host cells, by preference microorganisms, particularly preferably bacteria, that contain them, and expressing therein a contained nucleic acid. In various embodiments, the vectors described herein thus also contain regulatory elements that control expression of the nucleic acids encoding a polypeptide of the invention. Expression is influenced in particular by the promoter or promoters that regulate transcription. Expression can occur in principle by means of the natural promoter originally located in front of the nucleic acid to be expressed, but also by means of a host-cell promoter furnished on the expression vector or also by means of a modified, or entirely different, promoter of another organism or of another host cell. In the present case at least one promoter for expression of a nucleic acid as contemplated herein is made available and used for expression thereof. Expression vectors can furthermore be regulated, for example by way of a change in culture conditions or when the host cells containing them reach a specific cell density, or by the addition of specific substances, in particular activators of gene expression. One example of such a substance is the galactose derivative isopropyl-beta-D-thiogalactopyranoside (IPTG), which is used as an activator of the bacterial lactose operon (lac operon). In contrast to expression vectors, the contained nucleic acid is not expressed in cloning vectors.

In a further aspect, the invention is also directed to a host cell, preferably a non-human host cell, containing a nucleic acid as contemplated herein or a vector as contemplated herein. A nucleic acid as contemplated herein or a vector containing said nucleic acid is preferably transformed into a microorganism, which then represents a host cell according to an embodiment. Methods for the transformation of cells are established in the existing art and are sufficiently known to the skilled artisan. All cells are in principle suitable as host cells, i.e. prokaryotic or eukaryotic cells. Those host cells that can be manipulated in genetically advantageous fashion, e.g. as regards transformation using the nucleic acid or vector and stable establishment thereof, are preferred, for example single-celled fungi or bacteria. In addition, preferred host cells are notable for being readily manipulated in microbiological and biotechnological terms. This refers, for example, to easy culturability, high growth rates, low demands in terms of fermentation media, and good production and secretion rates for foreign proteins. The polypeptides can furthermore be modified, after their manufacture, by the cells producing them, for example by the addition of sugar molecules, formylation, amination, etc. Post-translation modifications of this kind can functionally influence the polypeptide.

Further embodiments are represented by those host cells whose activity can be regulated on the basis of genetic regulation elements that are made available, for example, on the vector, but can also be present a priori in those cells. They can be stimulated to expression, for example, by controlled addition of chemical compounds that serve as activators, by modifying the culture conditions, or when a specific cell density is reached. This makes possible economical production of the proteins contemplated herein. One example of such a compound is IPTG, as described earlier.

Preferred host cells are prokaryotic or bacterial cells. Bacteria are notable for short generation times and few demands in terms of culturing conditions. As a result, economical culturing methods resp. manufacturing methods can be established. In addition, the skilled artisan has ample experience in the context of bacteria in fermentation technology. Gram-negative or Gram-positive bacteria may be suitable for a specific production instance, for a wide variety of reasons to be ascertained experimentally in the individual case, such as nutrient sources, product formation rate, time requirement, etc.

Host cells contemplated herein can be modified in terms of their requirements for culture conditions, can comprise other or additional selection markers, or can also express other or additional proteins. They can, in particular, be those host cells that transgenically express multiple proteins or enzymes.

The host cell can, however, also be a eukaryotic cell, which is characterized in that it possesses a cell nucleus. A further embodiment is therefore represented by a host cell which is characterized in that it possesses a cell nucleus. In contrast to prokaryotic cells, eukaryotic cells are capable of post-translationally modifying the protein that is formed. Examples thereof are fungi such as Actinomycetes, or yeasts such as Saccharomyces or Kluyveromyces. This may be particularly advantageous, for example, when the proteins, in connection with their synthesis, are intended to experience specific modifications made possible by such systems. Among the modifications that eukaryotic systems carry out in particular in conjunction with protein synthesis are, for example, the bonding of low-molecular-weight compounds such as membrane anchors or oligosaccharides.

The host cells contemplated herein are cultured and fermented in a usual manner, for example in discontinuous or continuous systems. In the former case a suitable nutrient medium is inoculated with the host cells, and the product is harvested from the medium after a period of time to be ascertained experimentally. Continuous fermentations are notable for the achievement of a flow equilibrium in which, over a comparatively long period of time, cells die off in part but are also in part renewed, and the protein formed can simultaneously be removed from the medium.

Host cells contemplated herein are preferably used to manufacture the polypeptides described herein.

A further aspect of the invention is therefore a method for manufacturing a polypeptide as described herein, comprising culturing a host cell contemplated herein; and isolating the polypeptide from the culture medium or from the host cell. Culture conditions and mediums can be selected by those skilled in the art based on the host organism used by resorting to general knowledge and techniques known in the art.

In a still further aspect, the present invention relates to the use of polypeptides described above for protein ligation, in particular for cyclizing one or more peptide(s).

Also encompassed is the use of polypeptides that comprise, consist essentially of or consist of

-   (i) any one of the amino acid sequences as set forth in SEQ ID     Nos:3-109; -   (ii) an amino acid sequence that shares at least 60, preferably at     least 70, more preferably at least 80, most preferably at least 90%     sequence identity with any one of the amino acid sequences of (i)     over its entire length; -   (iii) an amino acid sequence that shares at least 80, preferably at     least 90, more preferably at least 95% sequence homology with any     one of the amino acid sequences of (i) over its entire length; or -   (iv) a fragment of any one of (i)-(iii), wherein said fragment has     ligase/cyclase activity, for ligating at least two peptides or     proteins or cyclizing a peptide or protein.

In various embodiments of such uses, the polypeptides according to (i)-(iv) based on the amino acid sequences as set forth in SEQ ID Nos. 3-109 are polypeptides based on SEQ ID NO:1, such as those described above. This relates in particular to the conserved amino acid residues N, H and C at positions corresponding to positions 19, 124 and 166 of SEQ ID NO:1 and/or their activity and functionality.

It is understood that while the uses of the enzymes described herein are described in the following by reference to peptide substrates, they can similarly be used for the corresponding polypeptides or proteins. The invention thus also covers embodiments where polypeptides or proteins are used as substrates. These polypeptides or proteins can comprise the structural motifs as described below in the context of peptide substrates. Also encompassed are embodiments, where peptide fragments, such as fragments of human peptide hormones that retain functionality, or peptide derivatives, such as (backbone) modified peptides, including, for example, thiodepsipeptides, are utilized. Accordingly, the present invention also covers fragments and derivatives of the peptide substrates disclosed herein.

In various embodiments the peptide to be ligated or cyclized can be any peptide, typically at least 10 amino acids in length, as long as it contains a recognition and ligation sequence that is recognized, bound and ligated by the ligase/cyclase. This amino acid sequence of the peptide to be ligated or cyclized may comprise the amino acid residue N or D, preferably N. In various embodiments, the peptide to be cyclized comprises the amino acid sequence (X)_(o)N/D(X)_(p), with X being any amino acid, o being an integer of 1 or more, preferably 2 or more, and p being an integer of 1 or more, preferably of 2 or more. In a preferred embodiment, (X)_(p) is H(X)_(r)or HV(X)_(r). with r being 0 or an integer of 1 or more. In more preferred embodiments, the peptide comprises the amino acid sequence(X)_(o)NH or (X)_(o)NHV. Said amino acid sequence is preferably located at or near the C-terminus of the peptide to be ligated or cyclized, as all amino acids C-terminal to the N will be cleaved off during ligation/cyclization. Accordingly, in all afore-mentioned embodiments, p or r are preferably integers of up to 20, preferably up to 5. Particularly preferred are embodiments, where p is 2, with (X)_(p) preferably being HX or HV, or where r is 0.

In alternative embodiments, the peptide to be ligated or cyclized may comprise the amino acid sequence (X)_(o)N*/D*, wherein X is any amino acid, o is an integer of at least 2 and the C-terminal carboxy group (of the N or D residue) is replaced by a group of the formula —C(O)—N(R′)₂, with R′ being any residue, such as, for example, alkyl. In such embodiments, the terminal —C(O)OH group of the N or D residue, preferably the alpha-carboxy group in case of D, is modified to form the group —C(O)—N(R′)₂. These C-terminally amidated D or N residues are indicated herein by D* and N*, respectively. It has been found that the enzymes disclosed herein can cleave the amide group and ligate said N or D residue to the N-terminus of another peptide of interest or the N-terminus of the same peptide that comprises the N or D residue.

The N-terminal part of the peptide to be ligated preferably comprises the amino acid sequence X¹X²(X)_(q), wherein X can be any amino acid; X¹ can be any amino acid with the exception of Pro; X² can be any amino acid, but preferably is a hydrophobic amino acid, such as Val, Ile or Leu, or Cys; and q is 0 or an integer of 1 or more. Preferred are in the X¹ position in the following order: G=H>M=W=F=R=A=I=K=L=N=S=Q=C>T=V=U>D=E. “=” indicates that the respective amino acids are similarly preferred, while “>” indicates a preference of the amino acids listed before the symbol over the ones listed after the symbol. Preferred in the X² position are in the following order: L>V>I>C>T>W>A=F>Y>M>Q>S. Less preferred in the X² position are P, D, E, G, K, R, N and H. Particularly preferred in the X¹ position are G and H and in the X² position L, V, I and C, such as the dipeptide sequences GL, GV, GI, GC, HL, HV, HI and HC.

In preferred embodiments, the peptide to be ligated or cyclized thus comprises in N- to C-terminal orientation, the amino acid sequence X¹X²(X)_(q)(X)_(O)N/D(X)_(p), wherein X, X¹, X², o, p, and q are defined as above, with o preferably being at least 7. In various embodiments, (1) q is 0 and o is an integer of at least 7; and/or (2) X¹ is G or H; and/or (3) X² is L, V, I or C; and/or (4) p is at least 2 but not more than 22, preferably 2-7, more preferably H(X)_(r) or HV(X)_(r), most preferably HX or HV. In various embodiments, (1) q is 0 and o is an integer of at least 7; and (2) X¹ is G or H; and (3) X² is L, V, I or C; and (4) p is at least 2 but not more than 22, preferably 2-7, more preferably H(X)_(r)or HV(X)_(r), most preferably HX or HV.

In various embodiments, the peptide to be cyclized is the linear precursor form of a cyclic cystine knot polypeptide, in particular a cyclotide. Cyclotides are a topologically unique family of plant proteins that are exceptionally stable. They comprise ˜30 amino acids arranged in a head-to-tail cyclized peptide backbone that additionally is restrained by a cystine knot motif associated with six conserved cysteine residues. The cystine knot is built from two disulfide bonds and their connecting backbone segments forming an internal ring in the structure that is threaded by the third disulfide bond to form an interlocking and cross braced structure. Superimposed on this cystine knot core motif are a well-defined beta-sheet and a series of turns displaying short surface-exposed loops.

Cyclotides express a diversity of peptide sequences within their backbone loops and have a broad range of biological activities. They are thus of great interest for pharmaceutical applications. Some plants from which they are derived are used in indigenous medicines, including kalata-kalata, a tea from the plant Oldenlandia affinis that is used for accelerating childbirth in Africa that contains the prototypic cyclotide kalata B1 (kB1). Their exceptional stability means that they have attracted attention as potential templates in peptide-based drug design applications. In particular, the grafting of bioactive peptide sequences into a cyclotide framework offers the promise of a new approach to stabilize peptide-based therapeutics, thereby overcoming one of the major limitations on the use of peptides as drugs.

In various embodiments, the peptide to be cyclized is thus 10 or more amino acids in length, preferably up to 50 amino acids, in some embodiments about 25 to 35 amino acids in length. The peptide to be cyclized may comprise or consist of the amino acid of the precursor of cyclotide kalata B1 from Oldenlandia affinis as set forth in SEQ ID NO:110.

In various embodiments, the peptide to be cyclized comprises or consists of the amino acid sequence (X)_(n)C(X)_(n)C(X)_(n)C(X)_(n)C(X)_(n)C(X)_(n)C(X)_(n)NHV(X)_(n) (SEQ ID NO: 161), wherein each n is an integer independently selected from 1 to 6 and X can be any amino acid. Such peptides are precursors of cyclic cystine knot polypeptides that form cystine bonds between the six cysteine residues, as described above, and which can be cyclized by the enzymes described herein by cleaving off the C-terminal HV(X)_(n) sequence and ligating the (then C-terminal) N residue to the N-terminal residue.

The peptides to be cyclized may, in various embodiments, include the linear precursors disclosed in US2012/0244575. This document is for this purpose incorporated herein by reference in its entirety.

In various additional embodiments, the peptides to be cyclized include, but are not limited to linear precursors of peptide toxins and antimicrobial peptides, such as conotoxins, thanatins (insect antimicrobial peptides) and histatins (human saliva antimicrobial peptides). Other peptides that may be cyclized are precursors of cyclic human or animal peptide hormones, including, but not limited to neuromedin, salusin alpha, apelin and galanin. Exemplary peptides include or consist of any one of the amino acid sequences set forth in SEQ ID Nos. 111-116 and 128-132.

Further peptides that can be ligated or cyclized using the enzymes and methods disclosed herein include, without limitation, Adrenocorticotropic Hormone (ACTH), Adrenomedullin, Intermedin, Proadrenomedullin, Adropin, Agelenin, AGRP, Alarin, Insulin-Like Growth Factor-Binding Protein 5, Amylin, Amyloid b-Protein, Amphipathic Peptide Antibiotic, LAH4, Angiotensin I, Angiotensin II, A-Type (Atrial) Natriuretic Peptide (ANP), Apamin, Apelin, Bivalirudin, Bombesin, Lysyl-Bradykinin, B-Type (Brain) Natriuretic Peptide, C-Peptide (insulin precursor), Calcitonin, Cocaine-and Amphetamine-Regulated Transcript (CART), Calcitonin Gene Related Peptide (CGRP), Cholecystokinin (CCK)-33, Cytokine-Induced Neutrophil Chemoattractant-1/growth-related oncogene (CINC), Colivelin, Corticotropin-Releasing Factor (CRF), Cortistatin,

C-Type Natriuretic Peptide (CNP), Decorsin, human neutrophil peptide-1 (HNP-1), HNP-2, HNP-3, HNP-4, human defensin HDS, HD6, human beta defensin-1 (hbdl), hbd2, hbd3, hbd4, Delta Sleep-Inducing Peptide (DSIP), Dermcidin-1L, Dynorphin A, Elafin, Endokinin C, Endokinin D, b-Lipotropin, g-Endorphin, Endothelin-1,Endothelin-2, Endothelin-3, Big-Endothelin-1, Big-Endothelin-2, Big-Endothelin-3, Enfuviritide, Exendin-4, MBP, Myelin

Oligodendrocyte Protein (MOG), Glu-fibrinopeptide B, Galanin, Galanin-like Peptide, Big Gastrin (Human), Gastric Inhibitory Polypeptide (GIP), Gastrin Releasing Peptide, Ghrelin,Glucagon, Glucagon-like peptide-1 (GLP-1), GLP-2, Growth Hormone Releasing Factor (GRF, GHRF), Guanylin, Uroguanylin, Uroguanylin Isomer A, Uroguanylin Isomer B, Hepcidin, Liver-Expressed Antimicrobial Peptide (LEAP-2),Humanin, Joining Peptide (rJP), Kisspeptin-10, Kisspeptin-54, Liraglutide, LL-37 (Human Cathelicidine), Luteinizing Hormone Releasing Hormone (LHRH), Magainin 1, Mastoparan, a-Mating Factor, Mast Cell Degranulating (MCD) Peptide, Melanin-Concentrating Hormone (MCH), a-Melanocyte Stimulating Hormone (alpha-MSH), Midkine, Motilin, neuroendocrine regulatory peptide 1 (NERP1), NERP2,Neurokinin A, Neurokinin B, Neuromedin B, Neuromedin C, Neuromedin S, Neuromedin U8, Neuronostatin-13, Neuropeptide B-29, Neuropeptide S (NPS), Neuropeptide W-30, Neuropeptide Y (NPY), Neurotensin, Nociceptin, Nocistatin, Obestatin, Orexin-A, Osteocalcin, Oxytocin, Catestatin, Chromogranin A, Parathyroid Hormone (PTH), Peptide YY, Pituitary Adenylate Cyclase Activating Polypeptide 38 (PACAP-38), Platelet Factor-4, Plectasin, Pleiotrophin, Prolactin-Releasing Peptide, Pyroglutamylated RFamide Peptide (QRFP), RFamide-Related Peptide-1, Secretin, Serum Thymic Factor (FTS), Sodium Potassium ATPase Inhibitor-1 (SPAI-1), Somatostatin, Somatostatin-28, Stresscopin, Urocortin, Substance P, Echistatin, Enterotoxin STp, Guangxitoxin-1E, Urotensin II, Vasoactive intestinal peptide(VIP), and Vasopressin as well as fragments and derivatives thereof. The afore-mentioned peptides may be of human or animal, such as rat, mouse, pig, origin. All of them all well-known to those skilled in the art and their amino acid sequences are readily available.

In various other embodiments, polypeptides or proteins of more than 50 amino acids length are used as cyclization substrates. In such a reaction, the polypeptide/protein may be cyclized by ligating its C- to its N-terminus.

In various embodiments, two or more peptides are ligated by the enzymes of the invention. This may include formation of macrocycles consisting of two or more peptides, preferable are macrocyclic dimers. The peptides to be ligated can be any peptides, as long as at least one of them contains a recognition and ligation sequence that is recognized, bound and ligated by the ligase/cyclase. Suitable peptides have been described above in connection with the cyclization strategy. The same peptides can also be used for ligation to another peptide that may be the same or different. One of the peptides to be ligated may for example be a polypeptide that has enzymatic activity or another biological function. The peptides to be ligated may also include marker peptides or peptides that comprise a detectable marker, such as a fluorescent marker or biotin. According to such embodiments, a polypeptide that has bioactivity can be fused to a detectable marker. In various embodiments, at least one of the peptides to be ligated has a length of 25 amino acids or more, preferably 50 amino acids or more (and thus may be a “polypeptide”, in the sense of the present invention).

The peptides to be ligated can comprise or consist of any of the amino acid sequences set forth in SEQ ID Nos. 117 to 127. Preferred peptides to be ligated to form (macrocyclic) dimers include the peptides having the amino acid sequence set forth in any one of SEQ ID Nos. 117-121. Preferred N-terminal peptides to be ligated (with one C-terminal peptide) to form a linear fusion peptide include the peptides having the amino acid sequence set forth in any one of SEQ ID Nos. 112, 115 and 117. Preferred C-terminal peptides to be ligated (with one N-terminal peptide) to form a linear fusion peptide include the peptides having the amino acid sequence set forth in any one of SEQ ID Nos. 113, 114 and 116.

The peptides to be ligated or cyclized can also be fusion peptides or polypeptides in which an Asx-containing tag has been C-terminally fused to the peptide of interest that is to be ligated or fused. The Asx-containing tag preferably has the amino acid sequence N/D(X)_(p), with X being any amino acid and o and p both being independently from each other an integer of 1 or more, preferably 2 or more. In a preferred embodiment, the tag comprises or consists of the (C-terminal) amino acid sequence NH or NHV. Alternatively, an amidated N or D (N* or D* as defined above) may be fused to the C-terminal end of the peptide or polypeptide to be ligated or fused. The other peptide to which this fusion peptide or polypeptide is ligated can be as defined above. Alternatively, the fusion peptide or polypeptide may be cyclized by forming a bond between its C- and N-terminus. In one embodiment, the fusion peptide or polypeptide may be green fluorescent protein fused to the C-terminal tag of the amino acid sequence NHV (SEQ ID NO: 133) and the ligated peptide may be a biotinylated peptide of the amino acid sequence GIGK(biotinylated)R (SEQ ID NO: 134). Generally, polypeptides and proteins that may be ligated to peptides, such as peptides bearing signaling or detectable moieties, or cyclized using the methods and uses described herein, include, without limitation antibodies, antibody fragments, antibody-like molecules, antibody mimetics, peptide aptamers, hormones, various therapeutic proteins and the like.

In various embodiments, the ligase activity is used to fuse a peptide bearing a detectable moiety, such as a fluorescent group, including fluoresceins, such as fluorescein isothiocyanate (FITC), or coumarins, such as 7-Amino-4-methylcoumarin, to a polypeptide or protein, such as those mentioned above. In various embodiments, the protein can be an antibody fragment, such as a human anti-ABL scFv, for example with the amino acid sequence set forth in SEQ ID NO:146, or an antibody mimetic, such as a darpin (designed ankyrin repeat proteins), for example a darpin specific for human ERK, for example with the amino acid sequence set forth in SEQ ID NO:147.

In still another aspect, the invention relates to a method for cyclizing a peptide, polypeptide or protein, the method comprising incubating said peptide, polypeptide, or protein with the polypeptides having ligase/cyclase activity described above in connection with the inventive uses under conditions that allow cyclization of said peptide.

In a still further aspect, the invention relates to a method for ligating at least two peptides, polypeptides or proteins, the method comprising incubating said peptides, polypeptides or proteins with the polypeptides described above in connection with the inventive uses under conditions that allow ligation of said peptides.

The peptides, polypeptides and proteins to be cyclized or ligated according to these methods are, in various embodiments, similarly defined as the peptides, polypeptides and proteins to be cyclized or ligated according to the above-described uses.

In the methods and uses described herein, the enzyme and the substrate can be used in a molar ratio of 1:100 or higher, preferably 1:400 or higher, more preferably at least 1:1000.

The reaction is typically carried out in a suitable buffer system at a temperature that allows optimal enzyme activity, usually between ambient (20° C.) and 40° C.

In the above-described methods and uses, the polypeptides having ligase/cyclase activity may be immobilized on a suitable support material. Suitable support materials include various resins that are used in chromatography columns and the like. The support may have the form of beads or may be the surface of larger structure, such as a microtiter plate. Immobilization allows for a very easy and simple contacting with the substrate, as well as easy separation of enzyme and substrate after the synthesis. If the polypeptide with the enzymatic function is immobilized on a solid column material, the ligation/cyclization may be a continuous process and/or the substrate/product solution may be cycled over the column.

Accordingly, the present invention, in one aspect, also covers a solid support material comprising the isolated polypeptide according to the invention immobilized thereon. The solid support material may comprise a polymer resin, preferably in particulate form, such as those mentioned above. The isolated polypeptide can be immobilized on the solid support material by covalent or non-covalent interactions.

In exemplary embodiments, the polypeptides having ligase/cyclase activity are glycosylated and may be immobilized by means of concanavalin A (Con A), a lectin (carbohydrate-binding protein) that is isolated from Canavalia ensiformis (jack bean). It binds specifically to a-D-mannose and a-D-glucose containing biomolecules, including glycoproteins and glycolipids. Said ConA protein is used in immobilized form on affinity columns to immobilize glycoproteins and glycolipids. Accordingly, in various embodiments, the isolated polypeptide having ligase/cyclase activity is glycosylated and non-covalently bound to a carbohydrate-binding moiety, preferably concanavalin A, coupled to the solid support material surface.

The solid support materials described above can be used for the on-column cyclization and/or ligation of at least one substrate peptide or in a method for the cyclisation or ligation of at least one substrate peptide, comprising contacting a solution comprising the at least one substrate peptide with the solid support material described above under conditions that allow cyclization and/or ligation of the at least one substrate peptide. The substrate peptides are those described above and include also the above polypeptide substrate.

The invention also encompasses a transgenic plant comprising a nucleic acid molecule encoding a polypeptide having protein ligase and/or cyclase activity as described herein. The polypeptide is preferably not naturally present in said plant. Accordingly, the present invention also features transgenic plants that express a heterologous polypeptide according to the invention.

In various embodiments such transgenic plants may further comprise at least one nucleic acid molecule encoding one or more peptides to be cyclized or one or more peptides to be ligated. These may be peptides as defined above in connection with the uses and methods of the invention. In one embodiment, the peptide to be cyclized is a linear precursor form of a cyclic cystine knot polypeptide, for example like those defined above. These precursors of peptides or polypeptides to be cyclized may be naturally present in said plant but are preferably also artificially introduced, i.e. the nucleic acids encoding them are heterologous.

Such transgenic plants may, due to the co-expression of the enzyme and its substrate, therefore directly produce a cyclized peptide of interest.

All embodiments disclosed herein in relation to the polypeptides and nucleic acids are similarly applicable to the uses and methods described herein and vice versa.

The invention is further illustrated by the following non-limiting examples.

EXAMPLES

Materials. Z-AAN-AMC (N-carbobenzyloxy-Ala-Ala-Asn-7-amido-4-methylcoumarin) and peptide substrates were synthesized by GL Biochem (Shanghai). Oxidative folding of each peptide substrate was performed for 18 h at a peptide concentration of 30 mM in the buffer containing 50% acetonitrile, 100 mM ammonium bicarbonate, 3 mM reduced glutathione, pH 8.0. Jack bean legumain was purchased from Takara Bio (Japan). Native kB1 peptide was isolated from aerial parts of O. affinis and purified by using RP-HPLC. Legumain-specific LP-1 probe was provided by Matthew Bogyo (Stanford University).

Accession codes. The nucleotide sequence for butelase 1 has been deposited in the GenBank database under the accession number KF918345.

Example 1 In Vitro Screening of Asparaginyl Endopeptidase and Peptide Cyclase Activity

The asparaginyl endopeptidase (AEP) activity was determined by using the fluorogenic substrate Z-Ala-Ala-Asn-AMC (Z-AAN-AMC), a fluorogenic substrate selective for legumains (Kembhavi, A. A., Buttle, D. J., Knight, C. G. & Barrett, A. J. The two cysteine endopeptidases of legume seeds: purification and characterization by use of specific fluorometric assays. Arch. Biochem. Biophys. 303, 208-213 (1993); Sojka, D. et al. IrAE—An asparaginyl endopeptidase (legumain) in the gut of the hard tick Ixodes ricinus. Int. J. Parasitol. 37, 713-724 (2007), at a concentration of 100 mM in buffer A. Emitted fluorescence was measured with an excited wavelength of 380 nm and emission wavelength of 460 nm.

In a first experiment, the crude extract of C. ternateawas incubated with Z-AAN-AMC under the above-described conditions. A large increase in fluorescence intensity at 460 nm was observed indicating the presence of a putative legumain.

Then the cyclase activity was assayed. Generally, in vitro cyclization assays were performed in 50-ml reaction mixtures containing buffer A, 0.125 mM butelase 1 and varying peptide concentrations (0.5 to 400 mM). The enzyme concentration was estimated by UV absorbance at 280 nm. Each reaction was performed in triplicate at 37° C. and quenched by adding 5 ml of 1 M HCl solution. The peptides were separated by using a reversed-phase C18 analytical column (150×2.1 mm, Vydac) on a Nexera UHPLC system (Shimadzu). The cyclization velocities were calculated by converting the HPLC-peak areas of remained linear precursors or the cyclized products into concentrations. The identity of each HPLC peak was analyzed by MALDI-TOF MS and MS/MS (ABI 4800 MALDI TOF/TOF).

The cyclase activity of the crude extract of C. ternatea was assayed using the peptide substrate kB1-NHV (SEQ ID NO:110), a 31-residue, linear and oxidatively folded form of the cyclotide kB1 with the His-Val sequence at the C-terminus as the propeptide (Table 1 and FIG. 1). Kalata B1(kB1), the prototypic cyclotide found in Oldenlandia affinis but not in C. ternatea, was selected as the substrate in our assays to distinguish it from native cyclotides produced by C. ternatea. The His-Val motif is conserved in the cyclotide precursors of C. ternatea and a C-terminal dipeptide has been shown to be sufficient for the biosynthesis of cyclotides (Nguyen, G. K., Lim, W. H., Nguyen, P. Q. & Tam, J. P. Novel Cyclotides and Uncyclotides with Highly

Shortened Precursors from Chassalia chartacea and Effects of Methionine Oxidation on Bioactivities. J. Biol. Chem. 287, 17598-17607 (2012). Conlan, B. F. et al. Insights into Processing and Cyclization Events Associated with Biosynthesis of the Cyclic Peptide Kalata B1. J. Biol. Chem. 287, 28037-28046 (2012)). Treatment of kB1-NHV with the extract of C. ternatea yielded a new peptide which matched the calculated mass of native cyclic kB1 (FIG. 2a,b ). This peptide product was further confirmed as cyclic kB1 by (1) co-elution with native cyclic kB1 in RP-HPLC (FIG. 3), (2) tryptic digestion which resulted in a mass increase of 18 Da suggesting a cyclic backbone, and MS/MS analysis confirming the kB1 sequence and Asn-Gly as the ligation site (FIGS. 4), and (3) 1D NMR which showed identical chemical shifts for the cyclized peptide and native cyclic kB1 (FIG. 5). For the 1D NMR spectra of kalata B1, native and butelase-cyclized kB1 peptides were prepared in 95% H₂O/5% D₂O at 0.1 mM concentration, pH 4.3. 1D ¹H spectra of both peptides were recorded on a 600 MHz NMR spectrometer (Bruker) equipped with a cryo-probe. These results indicate the presence of a putative ligase capable of peptide macrocyclization in the crude extract of C. ternatea.

TABLE 1 Cyclization yields of peptide  substrates mediated by butelase 1 Peptide  Substrate Time Yield (SEQ ID NO:) Sequence (h) (%) kB1-NHVIA  GLPVCGETCVGGTCNTPGCTCSW 3 >95 (137) PVCTRNHVIA kB1-NHVI  GLPVCGETCVGGTCNTPGCTCSW 2 >95 (136) PVCTRNHVI kB1-NHV  GLPVCGETCVGGTCNTPGCTCSW 0.8 >95 (110) PVCTRNHV kB1-NH  GLPVCGETCVGGTCNTPGCTCSW 4  <5 (138) PVCTRNH kB1-N*  GLPVCGETCVGGTCNTPGCTCSW 4 <10 (139) PVCTRN* kB1-DHV  GGLPVCGETCVGGTCNTPGCTCS 4 <10 (140) WPVCTRDHV kB1-AHV  GLPVCGETCVGGTCNTPGCTCSW 4  <1 (141) PVCTRAHV kB1-QHV  GLPVCGETCVGGTCNTPGCTCSW 4  <1 (142) PVCTRQHV kB1-EHV  GLPVCGETCVGGTCNTPGCTCSW 4  <1 (143) PVCTREHV SA-kB1-NHV^(a) GLPVCGETCVGGTCNTPGCTCSW 0.2 >95 (110) PVCTRNHV SFTI-NHV  GRCTKSIPPICFPNHV 0.8 >95 (135) SFTI-DHV  GRCTKSIPPICFPDHV 4 <10 (144) Assays were performed at 37° C. and an enzyme-to-peptide ratio of 1:400 (0.125 μM butelase 1:50 μM peptide). *indicates the amidated peptide at the C-terminus. ^(a)S-carbamidomethylated kB1-NHV.

Example 2 Isolation, Purification, Identification and Characterization of Butelase 1

Attempts to isolate the peptide ligase guided by Z-AAN-AMC were unsuccessful. Fractions giving strong fluorescence intensity after HPLC separation of the crude extract were unable to cyclize kB1-NHV. Instead, a peptide corresponding to the linear form of kB1 with His-Val being hydrolyzed was observed. All HPLC-separated fractions were then directly screened using kB1-NHV as the substrate, and cyclase activity was found in fractions lacking fluorescence (FIG. 2c ). This result demonstrates that the cyclase activity is separate from the AEP activity. As a control, commercial jack bean legumain was unable to cyclize kB1-NHV and generated only the linear form of kB1 (FIG. 2d ).

The putative ligase was purified in several chromatographic steps to give a single protein band of 38 kDa on SDS-PAGE (FIG. 6a ). For the isolation and purification 300 g pods of C. ternatea were homogenized with 500 ml of extraction buffer (20 mM sodium phosphate, 1 mM EDTA, 1 mM PMSF, 5 mM b-mercaptoethanol (b-ME), pH 6.0). The extraction was conducted at 4° C. to minimize protein degradation. The homogenate was centrifuged and filtered to remove plant debris. Ammonium sulfate was added to the supernatant to reach 20% saturation. The precipitated proteins were discarded and ammonium sulfate was continually added to the supernatant to reach 85% saturation. After centrifugation, the supernatant was discarded and the precipitated proteins were redissolved in 300 ml of extraction buffer. The dissolved sample was dialyzed overnight against 6 l of extraction buffer using a 10 kDa cut-off dialysis tubing. The dialyzed sample was centrifuged and filtered to give the crude extract of C. ternatea. This crude extract was applied to a flash column containing 100 ml slurry of Q-Sepharose Fast Flow anion-exchange resin (GE Healthcare). The column was wash with 800 ml of buffer A (20 mM phosphate buffer, 1 mM EDTA, 5 mM b-ME, pH 6.0) and eluted with 400 ml of buffer B (20 mM sodium phosphate, 1 mM EDTA, 5 mM b-ME, 200 mM KCl, pH 6.0). The eluent was concentrated to a final volume of 3 ml using 10 kDa cut-off centrifugal filter units (Amicon Ultra, Millipore). The concentrated sample was subjected to size exclusion chromatography using a BioSuite HPLC column (300×21.5 mm, Waters). Fractions with peptide cyclase activity were pulled and further purified by anion-exchange chromatography using an analytical PolyWAX HPLC column (200×4.6 mm, PolyLC). The enzyme purity was analyzed by SDS-PAGE and silver staining. Approximate 0.4 mg butelase 1 can be obtained from 300 g of plant materials.

Purified butelase 1 was analyzed by SDS-PAGE under denaturing condition. The gel was silver stained and the protein band was excised and subjected to in-gel tryptic digestion as described previously (Gharandaghi, F., Weinberg, C. R., Meagher, D. A., Imai, B. S. & Mische, S. M. Mass spectrometric identification of proteins from silver-stained polyacrylamide gel: A method for the removal of silver ions to enhance sensitivity. Electrophoresis 20, 601-605 (1999)). In-gel tryptic digestion gave five dominant peptide fragments that were then sequenced by MALDI-TOF MS/MS (FIG. 7). These fragments were BLAST searched against the transcriptome data of C. ternatea provided by the Beijing Genomics Institute, and were found to match a single sequence of a novel protein designated as butelase 1 (FIG. 6c ). The enzyme remains stable with minimal loss of activity for 30 days at 4° C. It is relatively soluble in water of which a concentration of 10 mg/ml has been achieved.

Based on the EST sequences in the transcriptome of C. ternatea, butelase 1 was predicted to consist of 482 residues and have a mass of 53 kDa, whereas the purified active enzyme is approximately 38 kDa, suggesting that it is post-translationally modified by proteolytic processing (FIG. 6c ). Incubating butelase 1 with PNGase F or glycopeptidase A produced no change in the molecular weight, indicating that butelase 1 is not N-glycosylated (data not shown). A BLASTp search against the NCBI non-redundant protein database showed that butelase 1 shares high sequence homology with several members of the legumain family. Butelase 1 has the highest homology with a legumain-like protein from Glycine max (NCBI reference sequence: XP_003525979) and VmPE-1 from Vigna mungo (GenBank: BAA76744.1) with 71% and 70% sequence identity, respectively. This result strongly suggests that butelase 1 is a novel member of the legumain family. The enzymological classification of butelase 1 was further supported by its labeling with the fluorescent probe LP-1, an aza-Asn epoxide probe specific for legumains (FIG. 6b and FIG. 8) (Lee, J. & Bogyo, M. Development of Near-Infrared Fluorophore (NIRF)-Labeled Activity-Based Probes for in Vivo Imaging of Legumain. ACS Chem. Biol. 5, 233-243 (2010)).

Legumains are produced as inactive zymogens that undergo autoproteolytic activation to release the N- and C-terminal prodomains. Edman sequencing revealed VEGTR as the N-terminal sequence of butelase 1. The C-terminal processing site was predicted to occur between Asn383 and Ser384, which is based on the apparent molecular weight of 38 kDa, and the auto-cleavage site of other legumains such as proteinase B from Vicia sativa and jack bean legumain (FIG. 6c ) (Becker, C. et al. Purification, Cdna Cloning and Characterization of Proteinase-B, an Asparagine-Specific Endopeptidase from Germinating Vetch (Vicia-Sativa L) Seeds. Eur. J. Biochem. 228, 456-462 (1995); Abe, Y. et al. Asparaginyl Endopeptidase of Jack Bean-Seeds—Purification, Characterization, and High Utility in Protein-Sequence Analysis. J. Biol. Chem. 268, 3525-3529 (1993)).

MODELLER was used to construct a homology model of butelase 1 based on the zymogen of human legumain, the only member of the legumain family with a known crystal structure (Safi, A. & Blundell, T. L. Comparative protein modelling by satisfaction of spatial restraints. J. Mol. Biol. 234, 779-815 (1993); Dall, E. & Brandstetter, H. Mechanistic and structural studies on legumain explain its zymogenicity, distinct activation pathways, and regulation. Proc. Natl. Acad. Sci. U. S. A. 110, 10940-10945 (2013)). The zymogen of butelase 1 (V42-1468) shares 37.8% sequence identity with human legumain. The constructed model of butelase 1 agrees well with the template structure of human legumain with a RMSD of 0.352Å for the backbone C_(a) (FIG. 6d ).

Previous study defined the zymogen of human legumain into three structural parts: the AEP active domain, the active peptide region, and the legumain stabilization and activity modulation (LSAM) domain. The latter two domains are auto-cleaved during enzyme activation in human legumain. Similarly, the modeled structure of butelase 1 can also be divided into three parts: the putative AEP active domain (marine blue, V42-T318), the active peptide region (magenta, D319-N383) and the LSAM domain (gray, S385-1468, which is excluded in the final active form of butelase 1). Overall, the AEP active domain of butelase 1 retains 49.8% sequence identity (V42-T318) and displays a good structural alignment of the catalytic triad (Asn59, His165 and Cys207) with that of human legumain (FIG. 6d ).

The kinetics of butelase 1 as a peptide cyclase were determined by HPLC and MS analysis using two non-native linear peptide substrates derived from different plant families, the 31-residue kB1-NHV and the 16-residue SFTI-NHV(SEQ ID NO:135). Despite being non-native substrates with different lengths and sequences, butelase 1 efficiently cyclized these peptides in excellent yields (Table 1).

RP-HPLC traces of the cyclization reaction revealed that butelase 1 converted about 40% of kB1-NHV into cyclic kB1 within 6 min, and reached >95% conversion within 45 min, at an enzyme-to-peptide ratio of 1:400 (FIG. 9a ). The apparent kinetic parameters of butelase 1 for kB1-NHV calculated from Michaelis-Menten plot using GraphPad Prismare 2.28±0.05 s⁻¹ for k_(cat), 213±10 mM for K_(m) and 10,700 M⁻¹ s⁻¹ for catalytic efficiency (k_(cat)/K_(m)) (FIG. 9b ). In addition, a 58-residue, cyclodimer of kB1 (<10%) was observed at high substrate concentrations (>400 mM), suggesting that butelase 1 is able to perform intermolecular ligation and cyclization of long peptide (FIG. 10).

With SFT1-NHV, butelase 1 also showed >95% conversion yield with the k_(cat) of 0.6±0.02 s⁻¹, K_(m) of 51±4 mM, and catalytic efficiency of 11,700 M⁻¹ s⁻¹ (FIG. 9c ). These data suggest that butelase 1 could cyclize a wide range of peptide substrates.

Since both SFTI and kB1 exist in nature as cyclic peptides stabilized by disulfide bonds, it was then determined whether conformational assistance by disulfide bonds is required for the cyclization reaction by butelase 1. S-alkylation of the reduced kB1-NHV with iodoacetamide gave SA-kB1-NHV. Treatment of 50 mM S-alkylated peptide (SA-kB1-NHV) with 0.125 mM butelase 1 resulted in >95% conversion to its cyclic form within 12 min (Table 1). Kinetic analysis showed a 50-fold improvement in the catalytic efficiency of SA-kB1-NHV compared to kB1-NHV (FIG. 9d ). This result demonstrates that disulfide bonds are not required for peptide cyclization by butelase 1.

To investigate the requirement of the P1′ and P2′ positions of the C-terminal propeptide, four analogs of kB1-NHV were synthesized (Table 1). Analogs with the longer propeptides than kB1-NHV displayed a small decrease in the cyclization rates, with catalytic efficiencies of 4032 and 2971 M⁻¹ s⁻¹ for kB1-NHVI(SEQ ID NO:136) and kB1-NHVIA (SEQ ID NO:137), respectively (Table 1 and Table 2). In contrast, butelase 1 was significantly less efficient in cyclizing two truncated analogs lacking either Val or His-Val (SEQ ID NO:138; SEQ ID NO:139) with <10% cyclic kB1 yield after 4 h, and an incomplete reaction after 30 h (FIG. 11). This result indicates that a C-terminal HV dipeptide is necessary for an efficient cyclization reaction by butelase 1.

TABLE 2 Kinetic parameters of butelase 1 for various peptide substrates Peptide Substrate k_(cat) (s⁻¹) K_(m) (μM) k_(cat)/K_(m) (M⁻¹ s⁻¹) SA-kB1-NHV 17.08 ± 5    31.5 ± 8   542,000 kB1-NHV 2.28 ± 0.05 213 ± 10  10,700 kB1-NHVIA 0.38 ± 0.01 129 ± 9  2971 kB1-NHVI 0.25 ± 0.01 62 ± 5  4032 SFTI-NHV  0.6 ± 0.02 51 ± 4  10,700 MrIA conotoxin 2.2 ± 0.2 7.9 ± 2   278,000

To determine the substrate specificity of butelase 1 at the P1 position, analog substrates of kB1-NHV were prepared by individually replacing the conserved Asn residue with Ala or closely related residues such as Asp, Glu and Gln (Table 1; SEQ ID Nos. 140, 141, 142, 143). No cyclization of kB1-AHV, kB1-QHV or kB1-EHV was observed after incubating with butelase 1 for 4 h (FIG. 12). Butelase 1 was able to cyclize kB1-DHV, but at about a hundred-fold slower than kB1-NHV and with less than 10% cyclized product after 4 h. Similarly, we compared the activity of butelase 1 on SFT1-NHV and SFT1-DHV (SEQ ID NO:144). Butelase 1 cyclized both peptide substrates, but was significantly more efficient with SFTI-NHV than SFTI-DHV. These results demonstrate that a C-terminal NHV tripeptide tag is necessary and sufficient for cyclization by butelase 1.

To provide the evidence of generality, it was examined whether butelase 1 can cyclize non-plant-derived proteins using substrates derived from conotoxin (MrIA; SEQ ID NO:111), a thanatin analog (insect antimicrobial peptide; SEQ ID NO:112), and histatin-1a, histatin-1b, histatin-3a, and histatin-3b (human saliva antimicrobial proteins; SEQ ID Nos. 113-116) (Table 3). Butelase 1 efficiently cyclized all tested peptides.

TABLE 3 Ligation yields of  peptides tested for cyclization Yield Peptides Sequence (%) MrIA =  GVCCGYKLCHPCAGNHV 95 Conotoxin (SEQ ID NO: 111) Thanatin GISKKPVPIIYCNRRTGKCQRMNHV 95 analog (SEQ ID NO: 112) Histatin-1a SADSHEKRHHGYRRKFHEKHHSHRE 90 FPFYGDYGSNYLYDNHV (SEQ ID NO: 113) Histatin-1b GLPDSHEKRHHGYRRKFHEKHHSHR 90 EFPFYGDYGSNYLYDNHV (SEQ ID NO: 114) Histatin-3a GADSHAKRHHGYKRKFHEKHHSHRG 90 YRSNYLYDNHV (SEQ ID NO: 115) Histatin-3b GLDSHAKRHHGYKRKFHEKHHSHRG 90 YRSNYLYDNHV (SEQ ID NO: 116)

To determine why Z-AAN-AMC was not useful in assaying for butelase 1, 0.125 mM purified enzyme was incubated with 50 mM Z-AAN-AMC. No apparent increase in the fluorescence intensity was observed after incubating for 30 h, indicating that butelase 1 did not hydrolyze Z-AAN-AMC. RP-HPLC analysis showed that <3% hydrolyzed product was formed (FIG. 13). As a positive control, jack bean legumain completely hydrolyzed Z-AAN-AMC under the same experimental conditions. This result suggests that butelase 1 has evolved to function as a ligase rather than a protease.

The cyclodimerization of kB1 suggests that butelase 1 is able to mediate intermolecular peptide ligation. It is worthwhile to point out that the high sequence diversity of >24 native cyclotides isolated from C. ternatea also provides tantalizing hints that butelase 1 is a promiscuous enzyme with broad substrate specificity. To define the N-terminal specificity of an acceptor nucleophile, KALVINHV (SEQ ID NO:122) was used as a model peptide and evaluated its ligation efficiency with XIGGIR(X=any one of the 20 naturally occurring amino acids (G,A,V,L,I,F,Y,W,H,R,K,S,T,D,E,N,Q,P,C,M); SEQ ID NO:123). The reactions were performed in the presence of 0.1 mM butelase 1, 50 mM KALVINHV (SEQ ID NO: 122) and 1 mM XIGGIR (SEQ ID NO: 123). Butelase 1 efficiently mediated the intermolecular peptide ligation with broad specificity, accepting most natural amino acids at the P1″ position except for Pro and acidic amino acids such as Asp and Glu (FIG. 15a ). The ligation yields reached 60-80% within 10 min of incubation for most peptides with <5% hydrolysis of the asparaginyl bond observed.

To define the specificity at the P2″ position, a second peptide library was synthesized: LXGGIR (SEQ ID NO:124) (X=any one of the 20 naturally occurring amino acids). Butelase 1 exhibits a more stringent requirement at the P2″ as compared to the P1″ position and displays a high preference for hydrophobic amino acids, particularly Ile, Leu and Val (FIG. 15b ). This result also explains the high catalytic efficiency of butelase 1 for conotoxin and histatin-3.

In addition ligation activity was also tested for the peptides YRNHV (SEQ ID NO:125)+GLPVR (SEQ ID NO:126) and TRNHV (SEQ ID NO:127) +GLPVR (SEQ ID NO:126).The ligation yields reached 60 within 10 min of incubation.

To demonstrate the generality of butelase 1, five non-cysteine-containing peptide hormones with sizes ranging from 26 to 40 residues were selected. Four sequences were derived from human peptides (neuromedin U (SEQ ID NO:128), salusin a (SEQ ID NO:129), apelin (SEQ ID NO:131), and galanin (SEQ ID NO:132)) and one from rat (neuromedin U; SEQ ID NO:130) (Table 4). Human galanin and neuromedin U contain an intrinsic Asn residue, thus enabling “traceless” ligation without leaving any additional sorting sequences in the final cyclized products. For other peptides, an additional Asn-His-Val sequence was added at the C-terminus and a Gly or Gly-Ile was added at the N-terminus as the linker sequence. The cyclization reactions were performed in 50 μl reaction mixtures containing 50 μM peptides and 0.1 μM butelase 1 (0.002 molar equivalent) at 37° C. HPLC and mass spectrometry were used to monitor the reactions. Remarkably, butelase 1 achieved >95% cyclization yields within 5 min for all peptides tested (FIG. 16). The fact that these peptides were randomly selected and share no sequence homology suggests the promiscuity and mimimal substrate requirement of butelase 1.

TABLE 4 Peptide Sequence Origin Neuromedin U RVDEEFQSPFASQSRGYFLF H. sapiens RPRNHV (SEQ ID NO: 128) Salusin GISGALPPAPAAPRPALRAQ H. sapiens RAGPAGPGAKNHV (SEQ ID NO: 129) Neuromedin U GIKYKVNEYQGPVAPSGGFF R. norvegicus LFRPRNHV (SEQ ID NO: 130) Galanin GLTSGWTLNSAGYLLGPHAV H. sapiens GNHRSFSDKNHV (SEQ ID NO: 132) Apelin GLVQPRGSRNGPGPWQGGRR H. sapiens KFRRQRPRLSHKGPMPFNHV (SEQ ID NO: 131)

Next the kinetics of cyclization of these peptide substrates were examined. The apparent kinetic parameters of butelase 1 were calculated from Michaelis-Menten plot using GraphPad Prism (Table 5). The catalytic efficiencies fall in the range of 1×10⁵ to 1.3×10⁶ M⁻¹ s⁻¹ which is consistent with our previous study on cysteine-rich peptides. This result confirmed that disulfides, and in turn a folded structure maintained by multiple disulfides, are not required for the cyclization by butelase 1.

TABLE 5 Peptide k_(cat) (s⁻¹) K_(m) (uM) k_(cat)/K_(m) (M⁻¹ S⁻¹) Galanin 3.54 ± 0.31 34.2 ± 6.5  103,000 Apelin 5.78 ± 0.25 6.7 ± 1.4 859,000 Neuromedin ∪ 5.78 ± 0.36 8.7 ± 2.1 664,000 Rat neuromedin ∪ 26.55 ± 2.48  20.2 ± 5.9  1,314,000

In addition, a trial ligation of green fluorescent protein with a C-terminal NHV-tag (SEQ ID NO:133) with a short peptide GIGK(biotin)R (SEQ ID NO:134) was performed to demonstrate the application of butelase 1 for protein labeling. For the reaction, 50 μM GFP with NHV tag, 0.125 μM butelase 1 and 1 mM GIGK(biotin)R (SEQ ID NO: 134) were incubated for 30 minutes at 37° C. The results are shown in FIG. 17.

To demonstrate that butelase 1 can cyclize proteins, a modified GFP ending with Asn-His-Val motif at the C-terminus and starting with Gly-Ile at the N-terminus was constructed (SEQ ID NO:145). The cyclization reaction was carried in the presence of 25 μM GFP and 0.1 μM butelase 1 (0.004 molar equivalent). The cyclization reaction completed within 15 min with >90% yield as monitored by SDS page and high resolution ESI-MS (FIG. 18). For comparison, sortase-mediated cyclization of GFP required an incubation of 24 hours and 1 molar equivalent of sortase A. The catalytic rate of butelase 1 is thus nearly 10,000 faster than sortase A using GFP as a model protein. This result demonstrated that butelase 1 is a powerful ligase with promising potential and can provide an alternative method for cyclization of peptide and proteins.

To investigate the ability of butelase 1 for introducing a functional group, such as biotin and fluorophores to proteins, C-terminal and N-terminal ligation was performed and the results analyzed by different techniques. For C-terminal ligation, the substrates tested are ABL-Mono (synthetic human scFv fragment against ABL protein; SEQ ID NO:146), and ERK-Darp (synthetic human antibody mimetic (darpin) specific for ERK; SEQ ID NO:147) (Table 6). For N-terminal ligation, the substrates tested were an ubiquitin protein (SEQ ID NO:148), and peptide 1 (YKNHV, SEQ ID NO: 149) or a thioglycolic acid variant (thiodepsipeptide) thereof (YKN-thioglycolic acid-V).

TABLE 6 Peptide Sequence Vector GFP-NHV MHHHHHHSSGVDLGTENLYFQSMSKGEE pNIC28- (SEQ ID  LFTGVVPILVELDGDVNGHKFSVSGEGE Bsa4 NO: 133) GDATYGKLTLKFICTTGKLPVPWPTLVT TLTYGVQCFSRYPDHMKQHDFFKSAMPE GYVQERTIFFKDDGNYKTRAEVKFEGDT LVNRIELKGIDFKEDGNILGHKLEYNYN SHNVYIMADKQKNGIKVNFKIRHNIEDG SVQLADHYQQNTPIGDGPVLLPDNHYLS TQSALSKDPNEKRDHMVLLEFVTAAGIT LGMDELYKNHV ABL-Mono MHHHHHHSSGVDLGTENLYFQSMGGSGS — (SEQ ID SVSSVPTKLEVVDATPTSLKISWDAYYS NO: 146) SWQNVKYYRITYGETGGDSPVQEFTVPG YYSTATISGLKPGVDYTITVYAYDTFFP GYEPNSPISINYRTNHV ERK-Darp MHHHHHHSSGVDLGTENLYFQSMGSDLG — (SEQ ID KKLLEAARAGQDDEVRILMANGADVNAH NO: 147) DDQGSTPLHLAAWIGHPEIVEVLLKHGA DVNARDTDGWTPLHLAADNGHLEIVEVL LKYGADVNAQDAYGLTPLHLAADRGHLE IVEVLLKHGADVNAQDKFGKTAFDISID NGNEDLAEILQKLNHV Ubiquitin MGIMQIFVKTLTGKTITLEVEPSDTIEN pET3a analog VKAKIQDKEGIPPDQQRLIFAGKQLEDG (SEQ ID RTLSDYNIQKESTLHLVLRLRGGHHHHH NO: 148) H

To investigate the capability of butelase 1 for C-terminal ligation, ABL-Mono with 14469.2 Da MW and ERK-Darp with 20270.2 Da MW were incubated with a fluorescent containing peptide GIR-AMC (AMC =7-Amino-4-methylcoumarin) in the presence of butelase 1. The reactions were monitored by MS (FIG. 19). Peaks detected at 14718.4 Da and 20511.1 Da are the ligated products of ABL-Mono and ERK-Darp with the addition of GIR-AMC and removal of His, Val and water molecule. ERK-Darp reaches nearly 90% conversion yield after 20 minute incubation.

Due to the large MW of ERK-Darp, GFP-NHV and their ligated products with the FITC-labelled peptide FITC-GKNHV (SEQ ID NO:150), analysis by MS was not accurate enough. ESI-MS, with specialty in ionizing macromolecules (Ho et al., Clin Biochem. Rev. (2003) 24(1), 3-12), was used to examine the large ligated products. For the ligatino reaction, 50 μM ERK-Darp and 50 μM GFP-NHV were incubated with 1 mM FITC-GKNHV (SEQ ID NO: 150) and 50 nM butelase 1 for 10 minute at 42° C. The product samples for ESI-MS were first isolated by UPLC to reduce the salt concentration. The result of ESI-MS was analyzed by ESI prot 1.0 program. The MW of ERK-Darp obtained by ESI-MS is 20205±1.5 Da, with only 239 Da difference to the theoretical MW. The MW of putative ligated product is 20453±1.6 Da and this proves the successful protein ligation. The MW of GFP-NHV and the putative ligated product are 29720.0±0.7 Da and 29969.3±0.7 Da respectively (FIG. 20).

For the N-terminal ligation, the reaction conditions were: 100 μM ubiquitin, 0.1 μM butelase 1, 500 μM peptide 1, incubated at 42° C. The reaction yield was 82% after 150 minutes. The reaction was monitored by HPLC and MS (FIG. 21).

Peptide dendrimers have been shown to have increased activity due to increased binding affinity. To test the possibility of using butelase 1 as a ligase to generate dendrimeric peptides, ligation of model peptide YRNHV (SEQ ID NO:125) to dimeric peptide G2K (two GIG sequences linked by a K residue) was carried out (FIG. 22). 50 μM G2K, 20 nM butelase 1 and 250 μM YRNHV (SEQ ID NO: 125) peptide were incubated at 37° C. for 1 h. Mass spectrometry was used to monitor the reaction at the end of the incubation (FIG. 22). The result provides a proof-of-concept that butelase 1 is able to act as a ligase for the dimerization of peptides.

The dimerization capabilities were also tested with peptides GV-10, SV-10, HV-10, EV-10 and RV-10 (SEQ ID Nos. 117-121). The results are shown in Table 7.

TABLE 7 Dimerization and cyclization of small peptides Yield Peptides Sequence (%) GV-10 GLPPPIFNHV → Cyclo(GLPPPIFN)₂ 50 (SEQ ID  NO: 117) SV-10 SLPPPIFNHV → Cyclo(SLPPPIFN)₂ 50 (SEQ ID  NO: 118) HV-10 HLPPPIFNHV → Cyclo(HLPPPIFN)₂ 50 (SEQ ID  NO: 119) EV-9 EINSTEINHV → Cyclo(EINSTEIN),  20 (SEQ ID  EINSTEINEINSTEINHV NO: 120) RV-10 RVTRPVNHV → Cyclo(RVTRPVN),  20 (SEQ ID  Cyclo(RVTRPVN)₂ NO: 121)

Example 3 N-terminal Cyclization Specificity

To further study the N-terminal specificity of butelase 1 with respect to its cyclase activity, three peptide libraries were synthesized and tested for cyclization:

Peptide library 1: (SEQ ID NO: 157) XLYRRGRYLRRNHV Peptide library 2: (SEQ ID NO: 158) XRLYRGRYLRRNHV Peptide library 3: (SEQ ID NO: 159) GXLYRGRYLRRNHV

In the afore-mentioned peptide libraries X designates any one of the 20 natural amino acids, as defined above. The cyclized peptides have the same sequence as given above, with the exception that the C-terminal residues HV have been cleaved off and the C-terminal N covalently linked to the N-terminal amino acid of the respective peptide. The reaction was performed in the presence of 50 nM butelase 1, 50 μM peptide, 42° C. for 60 min. The results of this cyclization activity test are shown as cyclization yields of the three peptide libraries in FIG. 23 a)-c).

From this experiment, it can be concluded that when the P2″ residue (the residue at position 2 as calculated from N- to C-terminus)is any one of Leu/Val/Ile/Cys, then the P1″ residue (i.e. the

N-terminal residue at position 1) is not important, which is similar to the result we obtained from the intermolecular ligation of KALVINHV (SEQ ID NO: 122) with XIGGIR (SEQ ID NO: 123) (Example 2). Further, when the P1″ residue is Gly, then P2″ can be any residue and still allow efficient cyclization.

Example 4 Reversible Immobilization of Butelase 1 on Concanavalin A Resin for On-Column Peptide Cyclization

Concanavalin A (Con A) is a lectin (carbohydrate-binding protein) that is isolated from Canavalia ensiformis (jack bean). It binds specifically to α-D-mannose and α-D-glucose containing biomolecules, including glycoproteins and glycolipids. Butelase 1 was recombinantly expressed and isolated in glycosylated form as a protein of about 37 kDa (data not shown). It was immobilized onto ProSwift® ConA-1S affinity column (Thermo Scientific) through its carbohydrate moieties. The immobilized butelase 1 was fully functional and was able to catalyze the on-column cyclization of SFTI-1, kB1 (kalata B1) and conotoxin. The reaction was performed in the presence of 50 μg immobilized butelase 1 and 50 μM of peptide substrates. UPLC profile illustrating the cyclisation of (a) Conotoxin GV-17 (SEQ ID NO:111) (b) SFTI-NHV (SEQ ID NO:135) (c) kB1 (SEQ ID NO:110) is shown in FIG. 24. 

The invention claimed is:
 1. A solid support material comprising immobilized thereon an isolated polypeptide having protein ligase or cyclase activity comprising or consisting of (i) the amino acid sequence as set forth in SEQ ID NO: 1; (ii) an amino acid sequence that shares at least 95% sequence identity with the amino acid sequence set forth in SEQ ID NO: 1 over its entire length and comprising: 1) the amino acid residue N at the position corresponding to position 18 of SEQ ID NO: 1; 2) the amino acid residue H at the position corresponding to position 124 of SEQ ID NO: 1; and 3) the amino acid residue C at the position corresponding to position 166 of SEQ ID NO: 1; or (iii) a fragment of any one of (i)-(ii) comprising amino acids 10-200 of the amino acid sequence set forth in SEQ ID NO: 1; wherein the solid support material comprises a particulate polymer resin material; wherein the isolated polypeptide is immobilized on the solid support material by covalent or non-covalent interactions, wherein, if the isolated polypeptide is non-covalently immobilized on the solid support material, the isolated polypeptide is glycosylated and non-covalently bound to a carbohydrate- binding moiety coupled to the solid support material surface; and wherein immobilization of the isolated polypeptide allows for contacting with a substrate and ligation or cyclization reaction of the substrate by the isolated polypeptide.
 2. The solid support material of claim 1, wherein the isolated polypeptide comprises or consists of the amino acid sequence set forth in SEQ ID NO:
 2. 3. The solid support material of claim 1, wherein said isolated polypeptide can cyclize a given peptide with a yield efficiency of 80% or more.
 4. The solid support material of claim 3, wherein the yield efficiency is 90% or more.
 5. The solid support material of claim 1, wherein said isolated polypeptide can cyclize a given peptide with (i) a K_(m) of 500 μM or less; (ii) a k_(cat) of at least 0.05 s⁻¹; or (iii) both (i) and (ii).
 6. The solid support material of claim 1, wherein the isolated polypeptide is glycosylated.
 7. The solid support material of claim 5, wherein the isolated polypeptide is non-covalently bound to a carbohydrate-binding moiety coupled to the solid support material surface.
 8. The solid support material of claim 7, wherein the carbohydrate-binding moiety is concanavalin A.
 9. The solid support material of claim 1, wherein the solid support material is a particulate resin material for chromatography columns. 